Evidence map›Paper›PMID 33996692›Full record

ArticleFrontiers in pediatrics2021

Biomarker Potential of the Soluble Receptor for Advanced Glycation End Products to Predict Bronchopulmonary Dysplasia in Premature Newborns.

Hayato Go, Hitoshi Ohto, Kenneth E Nollet, Kenichi Sato, Kyohei Miyazaki, Hajime Maeda, Hirotaka Ichikawa, Mina Chishiki, Nozomi Kashiwabara, Yohei Kume and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Observational
  2. Cell Proliferation and Apoptosis-Key Players in the Lung Aging Process.International journal of molecular sciences · 2024
    Review
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Hayato GoDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hitoshi OhtoFukushima Medical University, Fukushima, Japan.
Kenneth E NolletDepartment of Blood Transfusion and Transplantation Immunology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kenichi SatoDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kyohei MiyazakiDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hajime MaedaDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hirotaka IchikawaDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Mina ChishikiDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Nozomi KashiwabaraDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yohei KumeDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kei OgasawaraDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Maki SatoDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Mitsuaki HosoyaDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Fukushima Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bronchopulmonary dysplasia (BPD) is a common cause of pulmonary disease in preterm infants. The soluble receptor for advanced glycation end products (sRAGE) is implicated in the development of various pulmonary diseases. The objectives of the current study were to investigate perinatal factors associated with serum sRAGE levels at birth and to establish whether serum sRAGE could be a biomarker for BPD. This retrospective single-center study was conducted at Fukushima Medical University Hospital's Department of Pediatrics Neonatal Intensive Care Unit from April 2014 to September 2020. Mechanically ventilated or oxygenated neonates born at <32 weeks gestational age and healthy control neonates were included in this study. Serum sRAGE levels in cord blood were measured using an enzyme-linked immunosorbent assay. Eighty-four preterm infants born at <32 weeks and 40 healthy infants were identified. The 84 born at <32 weeks were categorized as BPD (

Indexed as

biomarkerbronchopulmonary dysplasiapremature infantsrageserum

Identifiers

PMID33996692
PMCPMC8116889
OpenAlexW3159464871

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.